Regulatory Affairs Specialist

1 mese fa


Milano, Lombardia, Italia The Kraft Heinz Company A tempo pieno

Job Summary

We are seeking a highly skilled Regulatory Affairs Manager to join our team at The Kraft Heinz Company. As a key member of our Legal, Government and Regulatory department, you will be responsible for ensuring all product labels used by Kraft Heinz in Europe comply with food legislation, government guidelines and company policies with a special focus on Infant Feeding products and Foods for Medical Purposes.

Main Responsibilities

  • Review and approve label artwork to ensure it meets legislation requirements, with a focus on Infant Feeding products and Foods for Special Medical Purposes.
  • Approve advertising copy and external communications to ensure they are not misleading and conform to legislation.
  • Review recipes and ingredient specifications, ensuring compositional requirements are met, codes of practice adhered to and company policies complied with.
  • Support the business in the provision of label information relating to products sold in Europe.
  • Develop relevant knowledge of Kraft Heinz business processes, products and relevant legislation.

Requirements

  • University Degree in a scientific field.
  • At least 4-5 years experience dealing with regulatory, ideally within government authority, leading companies or consultancies.
  • Deep knowledge of the European Food legislation.
  • Strong proficiency in English; Italian is a plus.
  • EU Working Permit is necessary to proceed with this position.

Desirable Competencies

  • Team player - Achieving results is nice, but achieving results with the team is simply the best.
  • Ability to Simplify - We like to keep it simple. And to implement fast.
  • Communication Skills - People are easily exposed to senior management, no matter their level.
  • Curiosity, positivity & passion - You're curious, positive and enthusiastic.

What We Offer

  • An ambitious employer; we only want the best for you.
  • Flexible working policy.
  • Fixed term contract for parental cover.
  • Always room for new insights; if you have an idea, please let us know, and we can set it in action.


  • Milano, Lombardia, Italia Hover Senior Living Community A tempo pieno

    Job SummaryThe Regulatory Affairs Senior Specialist will be supporting the implementation, execution and management of the local regulatory activities in Italy ensuring regulatory compliance with local regulatory requirements and corporate policies.The Regulatory Affairs Senior Specialist supports interactions with the national Regulatory Authorities, i.e....


  • Milano, Lombardia, Italia Recordati A tempo pieno

    Job DescriptionRecordati is seeking a highly skilled Regulatory Affairs Specialist to join its international team. As a key member of the Corporate Regulatory Affairs department, you will be responsible for the management of regulatory activities for medicinal products for human use.Key Responsibilities:Preparation, review, and submission of relevant...


  • Milano, Lombardia, Italia Page Personnel A tempo pieno

    Job SummaryWe are seeking a highly motivated Regulatory Affairs Specialist to support our medical devices team.Main ResponsibilitiesAs a Regulatory Affairs Specialist, you will play a key role in ensuring compliance with regulatory requirements for our medical devices. Key responsibilities include preparing and submitting regulatory submissions to regulatory...


  • Milano, Lombardia, Italia W EXECUTIVE S.R.L. A tempo pieno

    Job Title: Regulatory Affairs ManagerCompany: W EXECUTIVE S.R.L.Location: MilanoAs a Regulatory Affairs Manager at W EXECUTIVE S.R.L., you will be responsible for ensuring that our company's products comply with all relevant laws and regulations. This includes developing and executing regulatory strategies, managing product registrations, and providing...


  • Milano, Lombardia, Italia Page Personnel A tempo pieno

    About the RoleWe are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to join our team at Page Personnel.


  • Milano, Lombardia, Italia Cpl Healthcare A tempo pieno

    Job Title: Associate Director, Regulatory Affairs - Medical Device/Post Market SurveillanceJob Type: Full Time, Permanent PositionLocation: HybridRemuneration: Attractive salary and packageCpl Healthcare is seeking an experienced Associate Director, Regulatory Affairs - Medical Device Lifecycle Management to join their team. This role offers a unique...


  • Milano, Lombardia, Italia Page Personnel A tempo pieno

    Regulatory Affairs Specialist Medical DevicesPage Personnel è alla ricerca di un Regulatory Affairs Specialist Medical Devices motivato e dettagliato per unirsi al nostro team. Il Regulatory Affairs Specialist Medical Devices svolgerà un ruolo chiave nell'assicurare la conformità con i requisiti regolatori per i dispositivi medici. Questo individuo...


  • Milano, Lombardia, Italia Page Personnel A tempo pieno

    Regulatory Affairs Specialist for Medical DevicesWe are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to support our medical device team. The ideal candidate will have a strong understanding of regulatory requirements and guidelines, including FDA regulations (21 CFR Part 820), ISO 13485, and other applicable standards.Key...


  • Milano, Lombardia, Italia Lights On Women (Low) A tempo pieno

    Job Title: Regulatory Affairs Specialist - EU Compliance ExpertJob Summary: We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Lights On Women (Low). The successful candidate will be responsible for monitoring the evolution of the regulatory context within the EU, particularly in the gas distribution market, and ensuring the...


  • Milano, Lombardia, Italia Parexel A tempo pieno

    Regulatory Affairs Director Job DescriptionWe are seeking a highly skilled and experienced Regulatory Affairs professional to lead our team's regulatory efforts. As a Director, you will be responsible for ensuring compliance with regulatory requirements and guidelines, providing guidance to project teams, and managing performance and development of staff...


  • Milano, Lombardia, Italia Randstad Italia spa A tempo pieno

    Ricerche per un Regulatory Operations Specialist presso Randstad Italia spa.Descrizione del lavoroLa nostra azienda, Randstad Italia spa, è alla ricerca di un Regulatory Operations Specialist per sostenere il nostro team di Regulatory Affairs.Il candidato ideale dovrà essere in grado di assicurare la gestione dei cambiamenti regolatori, comprese le...


  • Milano, Lombardia, Italia Pfizer A tempo pieno

    Job OverviewWe are seeking a skilled Regulatory Affairs Specialist to join our team in the early-phase oncology portfolio. This role will play a crucial part in ensuring regulatory compliance and advancing the development of new cancer treatments.


  • Milano, Lombardia, Italia W Executive S.R.L. A tempo pieno

    Job SummaryW Executive S.R.L. is seeking a highly skilled Regulatory Affairs Manager to join our team. The successful candidate will be responsible for developing and executing regulatory strategies and plans to ensure compliance with applicable laws, regulations, and standards.Main Responsibilities• Manage the registration of pharmaceutical products,...

  • Regulatory Affairs Expert

    4 settimane fa


    Milano, Lombardia, Italia Parexel A tempo pieno

    Unlock Your Potential in Regulatory AffairsParexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant (Associate Director level) with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecule. The ideal candidate will possess strong regulatory affairs experience, project...


  • Milano, Lombardia, Italia Cpl Healthcare A tempo pieno

    Job Title: Associate Director, Regulatory Affairs - Medical Device/ Post Market SurveillanceJob Type: Full Time, Permanent PositionLocation: HybridRemuneration: Attractive salary and packageCpl Healthcare is seeking an experienced Regulatory Affairs Director to join their team. The ideal candidate will have a sound understanding of new registrations and...


  • Milano, Lombardia, Italia Elanco A tempo pieno

    About this roleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Elanco. As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.In this role, you will be responsible for developing and implementing global regulatory...


  • Milano, Lombardia, Italia Page Personnel A tempo pieno

    About the RoleWe are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to support our client, a medical company that develops Class III, II, and I devices.Key ResponsibilitiesRegulatory SubmissionsPrepare and submit regulatory submissions to regulatory authorities, including 510(k) premarket notifications, Technical Files, Design...


  • Milano, Lombardia, Italia Cpl Healthcare A tempo pieno

    Job Title: Senior Regulatory Affairs ManagerJob Type: Full Time, Permanent PositionLocation: Italy (Milan) – HybridRemuneration: Attractive salary and packageCpl Healthcare is seeking a Senior Regulatory Affairs Manager to join our team. As a key member of our Regulatory Affairs department, you will be responsible for the strategic lifecycle management of...


  • Milano, Lombardia, Italia Page Personnel A tempo pieno

    About the RoleWe are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to play a key role in ensuring compliance with regulatory requirements for our medical devices. In this position, you will collaborate with internal teams to support product development, registration, and post-market compliance activities.Key...


  • Milano, Lombardia, Italia Pfizer A tempo pieno

    Job DescriptionAt Pfizer, we are committed to transforming patients' lives through breakthroughs in drug discovery and development.As a Europe Regulatory Affairs Specialist, you will play a critical role in leading and implementing EU regulatory strategies in agreement with key stakeholders. Your expertise will ensure timely submissions and approvals, while...